Ana Rita Jesus

Dr. Ana Rita Jesus

Faculdade de Ciências e Tecnologia, Universidade Nova de Lisboa, Lisboa, Portugal
orcid

Research Focus & Metrics

Academic Career Length

16Years (2011-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 April 2019 in European Journal of Pharmaceutics and Biopharmaceutics
Verified
Journal Article
Closed access
Ana Rita JesusAna Rita Jesus
Ana Rita Jesus
MSMário R. C. Soromenho
Mário R. C. Soromenho
LRLuís R Raposo
Luís R Raposo
JEJosé M.S.S. Esperança
José M.S.S. Esperança
Pedro BaptistaPedro Baptista
Pedro Baptista
PRPatrícia Matias Reis
Patrícia Matias Reis


1 August 2021 in Cryobiology
Verified
Journal Article
Open access
Ana Rita JesusAna Rita Jesus
Ana Rita Jesus
LMLiane Meneses
Liane Meneses
ADAna Rita C. Duarte
Ana Rita C. Duarte
APAlexandre Paiva
Alexandre Paiva
This work aimed at evaluating the potential of using natural deep eutectic systems (NADES) as cryoprotectant agents (CPAs). Several combinations between natural primary metabolites that have been identified in animals that live in extreme cold climates were prepared. All systems showed very little cytoxicity towards L929 cells at concentrations high as 1-2 M. Moreover, this cell line was highly tolerant to 10% (w/v) of NADES when compared to Me2SO. To test NADES as CPAs, two cell lines were used, L929 and HacaT cells. After freeze/thawing cycle, it was possible to observe that for L929 cells, NADES presented similar behaviour to Me2SO. For Hacat cell line a significant improvement on post-thawing recovery was observed. Moreover, the results presented herein showed that NADES do not need to be removed from the freezing media after thawing the cells, which is a great advantage of these materials. Additionally, we have shown that NADES can act as CPA when cells are frozen at -20 °C. In overall, the results demonstrate the high potential of NADES to be used in cryobiology as alternative CPAs.

1 January 2011 in Current Organic Chemistry
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Journal Article
Closed access
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Rui Galhano dos SantosRui Galhano dos Santos
Rui Galhano dos Santos
Ana Rita JesusAna Rita Jesus
Ana Rita Jesus
JCJoao M. Caio
Joao M. Caio
Amélia Pilar RauterAmélia Pilar Rauter
Amélia Pilar Rauter
C-Glycosylphenols and -polyphenols occur widely in nature and present a variety of biological properties, namely antitumor, antibacterial and antidiabetic activities. Synthetic access to such structures relies mainly on efficient methodologies for phenols C-glycosylation. In the past few years major advances have been described addressing the use of Fries rearrangement to obtain a diversity of C-glycosyl compounds. Herein we survey the glycosyl donors and the activators used for this reaction, covering both early work and recent developments in the area. Reaction mechanism and reaction outcome control, aiming at regio- and stereoselectivity are also discussed.


1 January 2014 in European Journal of Medicinal Chemistry
Verified
Journal Article
Closed access
SSStefan Schwarz
Stefan Schwarz
BSBianka Siewert
Bianka Siewert
Nuno Manuel XavierNuno Manuel Xavier
Nuno Manuel Xavier
Ana Rita JesusAna Rita Jesus
Ana Rita Jesus
Amélia Pilar RauterAmélia Pilar Rauter
Amélia Pilar Rauter
René CsukRené Csuk
René Csuk